At a Glance
- Tasks: Create clear, patient-friendly summaries of complex clinical trial results.
- Company: Join a mission-driven team focused on transparency in clinical research.
- Benefits: Enjoy a fully remote role with competitive salary and professional development.
- Why this job: Make clinical research accessible and impactful for patients and the public.
- Qualifications: Strong writing skills and familiarity with medical writing and EU regulations.
- Other info: Flexible working hours and a supportive team environment.
The predicted salary is between 36000 - 60000 £ per year.
Plain Language Summary (PLS) Specialist – EU CTR Compliance (Remote, UK-based)
Overview
Do you have a passion for making clinical research more accessible to patients and the public? Join a fast-growing team dedicated to producing clear, compliant plain language summaries (PLS) in line with the EU Clinical Trial Regulation (CTR).
Responsibilities
- Develop high-quality plain language summaries that explain complex trial results in clear, patient-friendly language.
- Ensure deliverables meet EU CTR compliance requirements and client standards.
- Partner with global pharmaceutical teams to align on content, timelines, and strategy.
- Incorporate patient and lay reviewer feedback into final deliverables.
- Stay up to date with evolving guidance and best practices in plain language writing.
Qualifications
- Strong medical writing background, ideally with direct experience in PLS development.
- Familiarity with EU CTR guidance and regulatory landscape.
- Exceptional writing and editing skills, with the ability to simplify complex science.
- Strong organisational skills and attention to detail.
- Life sciences degree (MSc/PhD desirable, but not essential with relevant experience).
Benefits
- 100% remote role with flexibility across the UK.
- Be part of a mission-driven team committed to transparency and patient engagement.
- Competitive salary, training, and professional development opportunities.
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Plain Language Summary (PLS) Specialist employer: Albion Rye Associates
Contact Detail:
Albion Rye Associates Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Plain Language Summary (PLS) Specialist
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that PLS Specialist role.
✨Tip Number 2
Show off your skills! Create a portfolio showcasing your best plain language summaries and any relevant writing samples. This will help us see your ability to simplify complex information, which is key for this role.
✨Tip Number 3
Prepare for interviews by brushing up on EU CTR compliance and recent trends in patient engagement. We want to see that you’re not just passionate but also knowledgeable about the field!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Plain Language Summary (PLS) Specialist
Some tips for your application 🫡
Show Your Passion: When you’re writing your application, let your passion for making clinical research accessible shine through. We want to see how much you care about helping patients understand complex trial results!
Tailor Your Writing: Make sure to tailor your application to highlight your experience in plain language writing and EU CTR compliance. We love seeing how your background aligns with what we do at StudySmarter!
Be Clear and Concise: Just like the summaries we create, your application should be clear and to the point. Avoid jargon and keep it simple – we appreciate straightforward communication!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity.
How to prepare for a job interview at Albion Rye Associates
✨Know Your Stuff
Make sure you brush up on the EU Clinical Trial Regulation (CTR) and its compliance requirements. Familiarise yourself with the latest guidance and best practices in plain language writing, as this will show your passion for making clinical research accessible.
✨Showcase Your Writing Skills
Prepare a portfolio of your previous work that highlights your ability to simplify complex scientific concepts. Be ready to discuss specific examples where you've developed plain language summaries or similar documents, and how you incorporated feedback from patients or lay reviewers.
✨Be Organised and Detail-Oriented
During the interview, demonstrate your strong organisational skills by discussing how you manage timelines and collaborate with teams. Share examples of how your attention to detail has positively impacted your work, especially in meeting client standards.
✨Engage with the Interviewers
Don’t hesitate to ask questions about the team’s approach to patient engagement and how they incorporate feedback into their work. This shows your interest in collaboration and aligns with the mission-driven nature of the role.